Affiliation:
1. University of Rochester, Department of Biology, Rochester, New York 14627
Abstract
Bacteriophage Mu DNA was labeled after induction in the presence of [2-
3
H]adenine or [8-
3
H]adenine. Both Mu
mom
+
·
dam
+
DNA and Mu
mom
−
·
dam
+
DNA have similar
N
6
-methyladenine (MeAde) contents, as well as similar frequencies of MeAde nearest neighbors. Both DNAs are sensitive to in vitro cleavage by R·
Dpn
I but resistant to cleavage by R·
Dpn
II. These results indicate that the
mom
+
protein does not alter the sequence specificity of the host
dam
+
methylase to produce MeAde at new sites. However, we have discovered a new modified base, denoted A
x
, in Mu
mom
+
·
dam
+
DNA; approximately 15% of the adenine residues are modified to A
x
. Although the precise nature of the modification is not yet defined, analysis by electrophoresis and chromatography indicates that the
N
6
-amino group is not the site of modification, and that the added moiety contains a free carboxyl group. A
x
is not present in Mu
mom
+
·
dam
+
or Mu
mom
−
·
dam
+
phage DNA or in cellular DNA from uninduced Mu
mom
+
·
dam
+
lysogens. These results suggest that expression of the
dam
+
and
mom
+
genes are required for the A
x
modification and that this modification is responsible for protecting Mu DNA against certain restriction nucleases. Mu
mom
+
·
dam
−
DNA and Mu
mom
−
·
dam
−
DNA contain a very low level of MeAde (ca. 1 MeAde per 5,000 adenine residues). Since the only nearest neighbor to MeAde appears to be cytosine, we suggest that the methylated sequence is 5′... C-A
*
-C... 3′ and that this methylation is mediated by the
Eco
K modification enzyme.
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
Cited by
45 articles.
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